ENST00000265104.5:c.8921G>C
MANE Select
|
ENSP00000265104.4:p.Gly2974Ala
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ENST00000681290.1:c.8876G>C
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ENSP00000505288.1:p.Gly2959Ala
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ENST00000265104.4:c.8921G>C
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ENSP00000265104.4:p.Gly2974Ala
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NM_001369.2:c.8921G>C
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NP_001360.1:p.Gly2974Ala
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XM_005248262.2:c.8876G>C
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XP_005248319.1:p.Gly2959Ala
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XM_011513990.1:c.8921G>C
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XP_011512292.1:p.Gly2974Ala
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XR_925598.1:n.9028-3504G>C
|
|
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XM_005248262.3:c.9029G>C
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XP_005248319.2:p.Gly3010Ala
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XM_017009177.1:c.9029G>C
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XP_016864666.1:p.Gly3010Ala
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XM_017009178.1:c.7934G>C
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XP_016864667.1:p.Gly2645Ala
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XM_017009179.2:c.7934G>C
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XP_016864668.1:p.Gly2645Ala
|
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XM_017009180.1:c.9029G>C
|
XP_016864669.1:p.Gly3010Ala
|
|
XM_017009181.1:c.9029G>C
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XP_016864670.1:p.Gly3010Ala
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XM_017009182.1:c.9029G>C
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XP_016864671.1:p.Gly3010Ala
|
|
XM_017009183.1:c.9029G>C
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XP_016864672.1:p.Gly3010Ala
|
|
XM_017009184.1:c.9029G>C
|
XP_016864673.1:p.Gly3010Ala
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XM_017009185.1:c.4118G>C
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XP_016864674.1:p.Gly1373Ala
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XM_017009186.1:c.3671G>C
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XP_016864675.1:p.Gly1224Ala
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XM_017009188.1:c.3008G>C
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XP_016864677.1:p.Gly1003Ala
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XM_024454388.1:c.7934G>C
|
XP_024310156.1:p.Gly2645Ala
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XM_024454389.1:c.7523G>C
|
XP_024310157.1:p.Gly2508Ala
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XR_001742034.1:n.8946-3504G>C
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|
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XR_001742035.1:n.8946-3504G>C
|
|
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NM_001369.3:c.8921G>C
MANE Select
|
NP_001360.1:p.Gly2974Ala
|
|